Gabriel Minárik

2.1k total citations
123 papers, 1.5k citations indexed

About

Gabriel Minárik is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Gabriel Minárik has authored 123 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 52 papers in Molecular Biology, 29 papers in Genetics and 23 papers in Oncology. Recurrent topics in Gabriel Minárik's work include Cancer Cells and Metastasis (18 papers), Prenatal Screening and Diagnostics (15 papers) and Fetal and Pediatric Neurological Disorders (11 papers). Gabriel Minárik is often cited by papers focused on Cancer Cells and Metastasis (18 papers), Prenatal Screening and Diagnostics (15 papers) and Fetal and Pediatric Neurological Disorders (11 papers). Gabriel Minárik collaborates with scholars based in Slovakia, Czechia and United States. Gabriel Minárik's co-authors include Tomáš Szemes, Tatiana Sedláčková, Peter Celec, Gabriela Repiská, Ľudevít Kádaši, Michal Mego, Juraj Benca, Marián Karaba, Andrej Ficek and Daniel Pinďák and has published in prestigious journals such as Journal of Clinical Oncology, Bioinformatics and PLoS ONE.

In The Last Decade

Gabriel Minárik

118 papers receiving 1.5k citations

Peers

Gabriel Minárik
Reza Mastery Farahani Iran
Zhiqin Wang China
Carlos Alberto Moreira‐Filho Brazil
Yan Gao China
Paulo César Maiorka Brazil
Allerdien Visser Netherlands
Charlie Xiang United States
Li Yang China
Florence Bernex France
Loan Nguyen United States
Reza Mastery Farahani Iran
Gabriel Minárik
Citations per year, relative to Gabriel Minárik Gabriel Minárik (= 1×) peers Reza Mastery Farahani

Countries citing papers authored by Gabriel Minárik

Since Specialization
Citations

This map shows the geographic impact of Gabriel Minárik's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Gabriel Minárik with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Gabriel Minárik more than expected).

Fields of papers citing papers by Gabriel Minárik

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gabriel Minárik. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Gabriel Minárik. The network helps show where Gabriel Minárik may publish in the future.

Co-authorship network of co-authors of Gabriel Minárik

This figure shows the co-authorship network connecting the top 25 collaborators of Gabriel Minárik. A scholar is included among the top collaborators of Gabriel Minárik based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Gabriel Minárik. Gabriel Minárik is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Kráľová-Hromadová, Ivica, Eva Bazsalovicsová, Katarína Šoltýs, et al.. (2025). Genetic diversity and intercontinental dispersal of temperate and subarctic populations of Dibothriocephalus dendriticus (Cestoda; Diphyllobothriidea), a causative agent of dibothriocephalosis. International Journal for Parasitology. 55(6). 281–298. 2 indexed citations
2.
Mego, Michal, et al.. (2024). Association between glutathione S-transferases M1 expression and treatment outcome in germ cell tumor patients. Neoplasma. 71(4). 374–386. 2 indexed citations
3.
Piherová, Lenka, Hana Hartmannová, Gabriel Minárik, et al.. (2023). Trends in SARS-CoV-2 cycle threshold values in the Czech Republic from April 2020 to April 2022. Scientific Reports. 13(1). 6156–6156. 3 indexed citations
4.
Javor, Juraj, et al.. (2023). MMP2 rs243866 and rs2285053 Polymorphisms and Alzheimer’s Disease Risk in Slovak Caucasian Population. Life. 13(4). 882–882. 3 indexed citations
5.
Zaťková, Andrea, Zuzana Pös, Gabriel Minárik, et al.. (2023). Combination of expert guidelines-based and machine learning-based approaches leads to superior accuracy of automated prediction of clinical effect of copy number variations. Scientific Reports. 13(1). 10531–10531. 2 indexed citations
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Krumpolec, Patrik, Péter Baráth, Marian Grendár, et al.. (2023). The Potential of Liquid Biopsy in Detection of Endometrial Cancer Biomarkers: A Pilot Study. International Journal of Molecular Sciences. 24(9). 7811–7811. 2 indexed citations
8.
Karabinoš, Anton, et al.. (2022). Dilated cardiomyopathy is a part of the ARV1-associated phenotype: a case report. Journal of Medical Case Reports. 16(1). 98–98. 1 indexed citations
9.
Kushniarevich, Alena, Gabriel Minárik, Ľudevít Kádaši, et al.. (2021). A common founder effect of the splice site variant c.-23 + 1G > A in GJB2 gene causing autosomal recessive deafness 1A (DFNB1A) in Eurasia. Human Genetics. 141(3-4). 697–707. 3 indexed citations
10.
Jedličková, Ivana, Anna Přistoupilová, Lenka Nosková, et al.. (2020). Spinal muscular atrophy caused by a novel Alu‐mediated deletion of exons 2a‐5 in SMN1 undetectable with routine genetic testing. Molecular Genetics & Genomic Medicine. 8(7). e1238–e1238. 9 indexed citations
11.
Šoltýsová, Andrea, Tatiana Sedláčková, Dana Dvorská, et al.. (2020). Monosomy 3 Influences Epithelial-Mesenchymal Transition Gene Expression in Uveal Melanoma Patients; Consequences for Liquid Biopsy. International Journal of Molecular Sciences. 21(24). 9651–9651. 12 indexed citations
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Radvánszky, Ján, Eva Gonçalvesová, Folkert W. Asselbergs, et al.. (2019). Targeted next-generation sequencing in Slovak cardiomyopathy patients. Bratislavské lekárske listy/Bratislava medical journal. 120(1). 46–51. 6 indexed citations
14.
Budiš, Jaroslav, et al.. (2019). Non-invasive prenatal testing as a valuable source of population specific allelic frequencies. Journal of Biotechnology. 299. 72–78. 15 indexed citations
15.
Bazsalovicsová, Eva, Ivica Kráľová-Hromadová, Gabriel Minárik, et al.. (2018). Development of microsatellite loci in zoonotic tapeworm Dibothriocephalus latus (Linnaeus, 1758), Lühe, 1899 (syn. Diphyllobothrium latum) using microsatellite library screening. Molecular and Biochemical Parasitology. 225. 1–3. 10 indexed citations
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Lipov, Jan, et al.. (2016). ERVW-1 gene polymorphisms related to preeclampsia. Bratislavské lekárske listy/Bratislava medical journal. 117(6). 340–344. 2 indexed citations
18.
Kráľová-Hromadová, Ivica, Eva Bazsalovicsová, Gabriel Minárik, et al.. (2016). Population structure and dispersal routes of an invasive parasite, Fascioloides magna, in North America and Europe. Parasites & Vectors. 9(1). 547–547. 13 indexed citations
19.
Šoltýsová, Andrea, et al.. (2013). Thiopurine S-Methyltransferase Gene Polymorphisms in a Healthy Slovak Population and Pediatric Patients with Inflammatory Bowel Disease. Nucleosides Nucleotides & Nucleic Acids. 32(5). 239–246. 2 indexed citations
20.
Zmetakova, Iveta, Gabriel Minárik, Andrej Ficek, et al.. (2007). Identification of the deletions in the UGT1A1 gene of the patients with Crigler-Najjar syndrome type I from Slovakia.. PubMed. 26(4). 306–10. 3 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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